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Use of Remote Acyl Groups for Stereoselective 1,2-Cis-Glycosylation with Fluorinated Glucosazide Thiodonors

Abstract

Fluorinated glycans are valuable probes for studying carbohydrate-protein interactions at the atomic level. Glucosamine is a ubiquitous component of glycans, and the stereoselective synthesis of α-linked fluorinated glucosamine is a challenge associated with the chemical synthesis of fluorinated glycans. We found that introducing a 6-O-acyl protecting group onto 3-fluoro and 4-fluoro glucosazide thiodonors endowed them with moderate α-selectivity in the glycosylation of carbohydrate acceptors, which was further improved by adjusting the acceptor reactivity via O-benzoylation. Excellent stereoselectivity was achieved for 3,6-di-O-acyl-4-fluoro analogues. The glycosylation of threonine-derived acceptors enabled the stereoselective synthesis of the protected fluorinated analogue of α-GlcNAc-O-Thr, a moiety abundant in cell-surface O-glycans of protozoan parasite Trypanosoma cruzi. DFT calculations supported the involvement of transient cationic species which resulted from the stabilization of the oxocarbenium ion through O-6 acyl group participation.

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Article information


Submitted
22 May 2020
Accepted
29 Jun 2020
First published
29 Jun 2020

Org. Biomol. Chem., 2020, Accepted Manuscript
Article type
Paper

Use of Remote Acyl Groups for Stereoselective 1,2-Cis-Glycosylation with Fluorinated Glucosazide Thiodonors

V. Hamala, L. Červenková Šťastná, M. Kurfiřt, P. Curinova, M. Dracinsky and J. Karban, Org. Biomol. Chem., 2020, Accepted Manuscript , DOI: 10.1039/D0OB01065K

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